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A unified strategy for the biomimetic total synthesis of the spiroindimicin family of natural products was reported. Key transformations include a one‐pot two‐enzyme‐catalyzed oxidative dimerization of L‐tryptophan/5‐chloro‐L‐tryptophan to afford the bis‐indole precursors chromopyrrolic acid/5′,5′′‐dichloro‐chromopyrrolic acid, and regioselective C3′−C2′′ and C3′−C4′′ bond formation converting a common...
A unified strategy for the biomimetic total synthesis of the spiroindimicin family of natural products was reported. Key transformations include a one‐pot two‐enzyme‐catalyzed oxidative dimerization of L‐tryptophan/5‐chloro‐L‐tryptophan to afford the bis‐indole precursors chromopyrrolic acid/5′,5′′‐dichloro‐chromopyrrolic acid, and regioselective C3′−C2′′ and C3′−C4′′ bond formation converting a common...